Potential mutations that cause ARVC
收藏NIAID Data Ecosystem2026-03-13 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA771768
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资源简介：
We enrolled a 27-year-old Chinese patient with ARVC to make the genetic diagnosis. Whole-exome sequencing (WES) was performed on the genomic DNA obtained from this patient and Sanger sequence was performed for mutational analysis and confirmation
创建时间：
2021-10-16
